Canadian real-world experience of asciminib treatment in heavily pre-treated chronic myeloid leukemia (CML) patients who failed multiple lines of tyrosine kinase inhibitor (TKI) therapy

耐受性 髓系白血病 医学 累积发病率 内科学 酪氨酸激酶抑制剂 酪氨酸激酶 不利影响 胃肠病学 肿瘤科 队列 癌症 受体
作者
Fatima Khadadah,Sonia Cerquozzi,Harold J. Olney,Christina Fraga,Jill Dudebout,Anargyros Xenocostas,Nicholas Finn,Vincent Éthier,Mary Lynn Savoie,Lambert Busque,Kareem Jamani,Philip Kuruvilla,Carolyn Faught,Brian Leber,Rayan Kaedbey,Sarit Assouline,Dennis Dong Hwan Kim
出处
期刊:Leukemia Research [Elsevier BV]
卷期号:133: 107374-107374 被引量:9
标识
DOI:10.1016/j.leukres.2023.107374
摘要

Asciminib is a novel drug specifically targeting ABL myristoyl pocket in the ABL1 protein.Forty one patients with chronic myeloid leukemia treated with asciminib from 2018 to 2022 were reviewed and analyzed for the efficacy and tolerability of asciminib using real-world experience data.The median age was 60 years (range 17-90) with a past history of a cardiovascular event in 21 patients (51%). Patients were pretreated with a median of 3 previous tyrosine kinase inhibitors (range 1-5). After a median of 12 months of asciminib (range 3-41), major molecular response (MMR) rate was 39% (n = 11/28) and 42% (n = 5/12) at 6 and 12 months, respectively. Molecular response with 2 log reduction (MR2) was noted in 54% (n = 15/28) and 50% (n = 6/12) at 6 and 12 months. The cumulative incidence of MMR and MR2 was 46.3% and 66% at 12 months. Five patients discontinued asciminib due to treatment failure (n = 3) or thrombocytopenia (n = 2). There were no cardiovascular events. Out of 7 patients treated with high dose asciminib for T315I mutation, 5 patients achieved MMR or deeper response. The event-free survival was 63% at 12 months.This study confirmed clinical efficacy and tolerability of asciminib with real-world experience.
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